| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110561653-110561855 | Common:5; Rare:69 | ||||
| chr13:110615521-110615624 | Rare:43 | ||||
| chr13:110712986-110713285 | Common:2; Rare:134 | ||||
| chr13:110715350-110715569 | Common:1; Rare:86 | ||||
| chr13:110715576-110715889 | Common:1; Rare:167 | ||||
| chr13:111153569-111153720 | Common:2; Rare:69 | ||||
| chr13:113208637-113208712 | Rare:43 | ||||
| chr13:114234767-114235071 | Common:15; Rare:113 | ||||
| chr13:114281467-114281657 | Common:2; Rare:94 | ||||
| chr14:20333252-20333440 | Common:1; Rare:36 | ||||
| chr14:20343235-20343652 | Common:11; Rare:236 | ||||
| chr14:20413420-20413528 | Common:2; Rare:30 | ||||
| chr14:20455078-20455329 | Common:2; Rare:75 | ||||
| chr14:20684026-20684244 | Common:11; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684474-20684629 | Common:1; Rare:25; Clinvar (benign):1 |